Apparent mineralocorticoid excess Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Apparent mineralocorticoid excess (AME) is a rare form of pseudohyperaldosteronism characterized by very early-onset and severe hypertension, associated with low renin levels and hypoaldosteronism. (Orphanet Rare Disease Ontology, Orphanet_320)
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2 genes/proteins associated with the disease Apparent mineralocorticoid excess from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2 2.88009
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha 2.88009